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Aristaless Related Homeobox (ARX) (Middle Region) Peptide

ARX Hôte: Synthetic BP, WB
N° du produit ABIN8094953
168,15 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Aristaless Related Homeobox (ARX) (Middle Region) Peptide (ABIN8094953)

Antigène

Arx (ARX) (Aristaless Related Homeobox (ARX))

Source

  • 5
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Fonction

    ARX Peptide - middle region
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    This is a synthetic peptide designed for use in combination with anti-ARX antibody ( ARP31598_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Antigène

    Arx (ARX) (Aristaless Related Homeobox (ARX))

    Sujet

    Background Information: ARX gene is a homeobox-containing gene expressed during development. The expressed protein ARX contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy.This gene is a homeobox-containing gene expressed during development. The expressed protein contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alternative Symbols: ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRXS1, PRTS, CT121, EIEE1, MRX76, MRX87

    Poids moléculaire

    58kDa

    ID gène

    170302

    NCBI Accession

    NP_620689

    UniProt

    Q96QS3
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